Literature DB >> 871298

Experimental studies on cardiac muscle cell adaptation to insult.

G Rona, I Hüttner, J Dusek, M C Badonne.   

Abstract

Studies were carried out in rats on myocardial adaptation to injury produced by left coronary artery ligation. In the ischemic zone, open collaterals were present as shown by studies using the fine structural extracellular protein tracer, horseradish peroxidase (HRP). This phenomenon may explain the inhomogeneous cardiac muscle cell alteration in the early phase of coronarogenic myocardial injury. Reperfusion, as evidenced by the influx of HRP into the damaged cells, unmasked sarcolemmal membrane injury. Cardiac muscle cell stimulation modifies the binding of macromolecules to cell components and may influence the repair processes. In the surviving myocardium, correlative enzyme histochemical and ultrastructural studies demonstrated the development of alternative metabolic pathways and morphological signs of adaptation explaining increasing resistance of such cardiac muscle cells to subsequent insult.

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Year:  1977        PMID: 871298     DOI: 10.1007/bf01906364

Source DB:  PubMed          Journal:  Basic Res Cardiol        ISSN: 0300-8428            Impact factor:   17.165


  16 in total

1.  An infarct-like myocardial lesion and other toxic manifestations produced by isoproterenol in the rat.

Authors:  G RONA; C I CHAPPEL; T BALAZS; R GAUDRY
Journal:  AMA Arch Pathol       Date:  1959-04

2.  Protection, by coronary ligature, against isoproterenol-induced myocardial necroses.

Authors:  H SELYE; R VEILLEUX; S GRASSO
Journal:  Proc Soc Exp Biol Med       Date:  1960-06

3.  Protection of the ischemic myocardium. Introductory remarks.

Authors:  E Braunwald
Journal:  Circulation       Date:  1976-03       Impact factor: 29.690

4.  Colloidal lanthanum as a marker for impaired plasma membrane permeability in ischemic dog myocardium.

Authors:  S Hoffstein; D E Gennaro; A C Fox; J Hirsch; F Streuli; G Weissmann
Journal:  Am J Pathol       Date:  1975-05       Impact factor: 4.307

5.  Metabolic changes in infarcted and non-infarcted myocardium during the postinfarction period.

Authors:  S Gudbjarnason; K G Ravens; P Mathes
Journal:  Recent Adv Stud Cardiac Struct Metab       Date:  1972

6.  Myocardial resistance to isoprenaline in rats: variations with time.

Authors:  J Dusek; G Rona; D S Kahn
Journal:  J Pathol       Date:  1971-12       Impact factor: 7.996

7.  Myocardial resistance. A study of its development against toxic doses of isoproterenol.

Authors:  J Dusek; G Rona; D S Kahn
Journal:  Arch Pathol       Date:  1970-01

8.  Healing process in the marginal zone of an experimental myocardial infarct. Findings in the surviving cardiac muscle cells.

Authors:  J Dusek; G Rona; D S Kahn
Journal:  Am J Pathol       Date:  1971-03       Impact factor: 4.307

9.  Blood supply of the myocardium after temporary coronary occlusion.

Authors:  A Krug; G Korb
Journal:  Circ Res       Date:  1966-07       Impact factor: 17.367

10.  Permeability alteration of sarcolemmal membrane in catecholamine-induced cardiac muscle cell injury. In vivo studies with fine structural diffusion tracer horse radish peroxidase.

Authors:  M Boutet; I Hüttner; G Rona
Journal:  Lab Invest       Date:  1976-05       Impact factor: 5.662

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  1 in total

1.  Impaired sarcolemmal membrane permeability in reperfused ischemic myocardium. Ultrastructural tracer study.

Authors:  J P Camilleri; D Joseph; D Amat; J N Fabiani
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1980
  1 in total

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